Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,634 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,634 in last 12 months

Showing 80818100 of 13,398 recalls

DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Phenylephrine 2.5% Recalled by Isomeric Pharmacy Solution, LLC Due to Lack...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Methylprednisolone Acetate 80 mg/mL Recalled by Isomeric Pharmacy Solution,...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2017· Fagron, Inc

Recalled Item: Estrone Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...

The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2017· PharMedium Services, Llc

Recalled Item: Fentanyl Citrate (Preservative Free) 20 mcg per mL (2 Recalled by PharMedium...

The Issue: Labeling: Not Elsewhere Classified- Diluent used to compound product expired...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRADIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Cell Distributors

Recalled Item: Tears (Carboxymethylcellulose Sodium Solution) 0.5% Recalled by Cell...

The Issue: Labeling: Not elsewhere classified; product labeling lacks a NDC number, net...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRADIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRONE Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2017· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: Alka-Seltzer Gold (1000 mg Anhydrous citric acid Recalled by Bayer...

The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2017· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: Alka-Seltzer Original ( 325 mg Aspirin (NSAID) Recalled by Bayer HealthCare...

The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2017· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID) Recalled by Bayer...

The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Taro Pharmaceuticals...

The Issue: Failed Content Uniformity Specifications; out-of-specification (OOS) results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2017· Teva Pharmaceuticals USA

Recalled Item: PrednisoLONE Oral Solution USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Stability Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 28, 2017· Gary Wood

Recalled Item: hCG Body Shaper Recalled by Gary Wood Due to Marketed without an Approved...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis has found the product to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2017· Envy Me

Recalled Item: LaBri's Body Health Atomic Recalled by Envy Me Due to Undeclared Sibutramine

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2017· Novartis Pharmaceuticals Corp.

Recalled Item: Isopto Carpine (pilocarpine hydrochloride opthalmic solution) 4% Recalled by...

The Issue: Failed Impurities/Degradation Specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· GlaxoSmithKline, LLC

Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Aerosol Recalled by...

The Issue: Defective Delivery System: Elevated number of units with out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· Novartis Pharmaceuticals Corp.

Recalled Item: Pilocarpine Hydrochloride Ophthalmic Solution 4% Recalled by Novartis...

The Issue: Failed Impurities/Degradation Specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund